Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
  • C08H6/00—Macromolecular compounds derived from lignin, e.g. tannins, humic acids
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07G—COMPOUNDS OF UNKNOWN CONSTITUTION
  • C07G1/00—Lignin; Lignin derivatives
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
  • C08H8/00—Macromolecular compounds derived from lignocellulosic materials
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L97/00—Compositions of lignin-containing materials
  • C08L97/005—Lignin
• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
  • D21C1/00—Pretreatment of the finely-divided materials before digesting
  • D21C1/04—Pretreatment of the finely-divided materials before digesting with acid reacting compounds
• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
  • D21C3/00—Pulping cellulose-containing materials
  • D21C3/04—Pulping cellulose-containing materials with acids, acid salts or acid anhydrides
• • D—TEXTILES; PAPER
  • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
  • D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
  • D21C11/00—Regeneration of pulp liquors or effluent waste waters
  • D21C11/0007—Recovery of by-products, i.e. compounds other than those necessary for pulping, for multiple uses or not otherwise provided for
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
  • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]

Definitions

• the invention relates to a method for manu ⁇ facturing a lignin component. Further, the invention relates to a lignin component and a use of the lignin component. Further, the invention relates to a prod ⁇ uct .
• the objective of the invention is to disclose a new method for manufacturing a lignin component. Another objective of the invention is to produce a lig ⁇ nin component with improved properties and a product comprising the lignin component.
• the lignin component according to the present invention is characterized by what is presented in claims .
• Fig. 1 is a flow chart illustration of a method according to one embodiment of the present in ⁇ vention
• Fig. 2 is a flow chart illustration of a method according to another embodiment of the present invention.
• Fig. 3 is a flow chart illustration of a method according to another embodiment of the present invention.
• Fig 4 is a flow chart illustration of a method according to another embodiment of the present in- vention.
• Fig. 5a and 5d show lignin structures in cakes of comparative lignin components
• Fig. 5b and 5c show lignin structures in cakes of lignin components according to the present invention
• Fig. 6 is a flow chart illustration of a method according to one embodiment of the present in ⁇ vention
• Fig. 7 is a flow chart illustration of a method according to another embodiment of the present invention.
• Fig. 8 shows a SEM-picture of lignin struc ⁇ ture in cake of one lignin component according to the present invention
• Fig. 9 shows a flow chart illustration of a method according to one embodiment of the present in ⁇ vention
• Fig. 10 shows a flow chart illustration of a method according to another embodiment of the present invention.
• Fig. 11 shows a device according to one embodiment of the present invention. DETAILED DESCRIPTION OF THE INVENTION
• a lig- nin component is made from lignin material by an acid treatment, the method comprising: forming a lignin component of lignin material by treating the lignin material in at least one acid treatment stage; and op ⁇ timizing process conditions by means of a combination of process parameters comprising retention time, tem ⁇ perature and pH level at the acid treatment stage so that the retention time is over 6 hours during at least one acid treatment stage.
• FIG. 1 One embodiment of the method of the present in ⁇ vention is shown in figure 1. Another embodiment of the method of the present invention is shown in figure 2. Another embodiment of the method of the present inven ⁇ tion is shown in figure 3. Another embodiment of the method of the present invention is shown in figure 4. Further, lignin structures in cakes of lignin compo ⁇ nents are shown in figures 5a - 5d.
• a lig ⁇ nin component is made from a lignin material (1) by a mild acid treatment.
• a lignin component (3) is formed of lignin material so that the lignin material (1) is treated in at least one acid treatment stage (2a, 2b) and the at least one acid treatment stage is optimized by means of a combi- nation of process parameters comprising retention time, e.g. long retention time, temperature, e.g. high temperature, and pH level, e.g. sufficient low, in or ⁇ der to decrease ash and/or carbohydrates in the lignin component, and preferably in order to remove undesired substance from the lignin component and to purify the lignin component.
• the invention is specially based on improving properties of the lignin component.
• the properties such as purity, dry solids content, filterability, amounts of carbohydrates and ash, of the lignin component can be improved. Further, odour in the lignin component can be decreased. Then it is provided the lignin component which is suitable to use in typical and special applications.
• a lignin material refers any material or composition containing lignin.
• the lignin material may contain one or more material components.
• suitable and desired additives can be added into the lignin material to form a desired lignin component.
• the lignin material in ⁇ cludes flash precipitated lignin.
• flash precipitated lignin is obtained after C0 2 - precipitation .
• flash precipitated lignin is formed as disclosed in patent application PCT/FI2011/050896.
• the lignin is precipitated from the black liquor by a continuous process with C0 2 at 3 - 8 bar overpressure.
• the lig ⁇ nin is separated by a flash precipitation lignin sepa- ration method, such as disclosed in patent application PCT/FI2011/050896.
• the lignin is flash precipitated lignin.
• flash precipitated lignin should be understood in this specification as lignin that has been precipi- tated from black liquor in a continuous process by de ⁇ creasing the pH of a black liquor flow, under the influence of an over pressure of 200 - 1000 kPa, down to the precipitation level of lignin using a carbon dioxide based acidifying agent, preferably carbon dioxide, and by suddenly releasing the pressure for precipitat ⁇ ing lignin.
• the residence time in the above method is under 300 s.
• the flash precipitated lignin particles, having a particle diameter of less than 2 ⁇ form agglomerates, which can be separated from black liquor using e.g. filtration.
• the flash precipitated lignin can be purified and/or activated if needed for the further processing.
• the flash precipitated lignin has many advantages, e.g. activity, dispersability, solu ⁇ bility, drainability and preservability .
• the lignin component is a flash precipitated kraft lignin.
• the flash precipitated kraft lignin is undrained. There ⁇ fore the lignin has higher activity, and the lignin can be re-dissolved.
• the lignin needs only a very sim- pie re-dispersing stage when it is added e.g. into an adhesive mixture.
• the flash precipitated kraft lignin has dry matter content of 50 - 80 %.
• the lignin material is treated chemically and/or mechanically before the at least one acid treatment stage of the present inven ⁇ tion.
• the lignin material is precipi- tated before the at least one acid treatment stage.
• the lignin material is re-slurried be ⁇ fore the at least one acid treatment.
• a lignin component means product formed from lignin material in at one or more stages.
• Term “lignin component” is already used after the first treatment stage.
• a carbohydrate refers any carbohydrates, especially hemicellulose.
• the at least one acid treatment stage is acid washing (2a) .
• an amount of ash can be decreased in the lig ⁇ nin component.
• filtera- bility of the lignin component can be enhanced.
• Fur ⁇ ther in the acid washing dry solids content of the lignin component can be improved.
• Improved dry solid content of filter cake leads to lower energy consumption in drying and to lower consumption of water in washing to reach same purity.
• dryer can be small ⁇ er, which leads to savings in investment. Savings in water consumption is important, since likely washing water must be circulated back to evaporation plant.
• certain dry solid content is needed to maintain processability of lignin cakes. For applications re ⁇ quiring no drying, for example burning, the low con- tent of water in filter cake is a benefit.
• the at least one acid treatment stage is acid hydrolysis (2b) .
• an amount of carbohydrates can be decreased in the lignin component.
• an amount of ash can be still decreased in the lignin component.
• lignin softens before or during acid hydrolysis; then carbohydrates can be removed from the lignin component and the lig- nin component can be purified.
• the softening is pref ⁇ erably performed slowly in correct temperature to pre- vent condensation of lignin and formation of char. The softening can be carried out at wide pH range.
• the lignin material (1) is treated at two acid treatment stages in which first stage is acid washing (2a) and second stage is acid hydrolysis (2b) .
• the first stage can be a typical acid washing.
• the second stage is a purifica ⁇ tion stage.
• the acid washing refers to any acid washing method.
• the acid washing is performed with H 2 S0 4 , other acid or other suitable acidifying chemical.
• the optimization of the invention affects positively consumption of H 2 S0 4 or other acid or other acidifying chemical.
• the acid hydrolysis refers to any acid hydrolysis method.
• the acid hydrolysis is performed by means of H 2 S0 4 , or oth ⁇ er suitable acidifying chemical, typically in the presence of water.
• the lignin material is treated in the at least one acid treatment stage with H 2 S0 4 .
• the method comprises two acid treatment method steps.
• the first step is a removal of ash and the second step is a removal of carbohydrates.
• the first step is a in ⁇ creasing of dry solids content in the lignin component and the second step is a removal of carbohydrates from the lignin component.
• the first step comprises a removal of ash and increasing of dry solids content in the lignin component, and the second step is a removal of carbohydrates from the lignin component.
• the method comprises a pre- treatment step before the at least one acid treatment stage.
• the lignin material is re- slurried in the pre-treatment step.
• the pre-treatment step is a softening step of lignin in which the lignin is softened and structure of the lignin is modified.
• An acid is able to hydrolyze carbohydrates in lignin after the softening step.
• each acid treatment stage of the invention a suitable combination of temperature, retention time and pH level is selected.
• the selected combi ⁇ nation varies based on acid washing or acid hydrolysis.
• the process conditions are selected such that lignin does not alternate into carbon or char during the acid treatment.
• long retention time is used in the acid treatment according to the invention.
• the retention time is over 1 hour.
• the retention time is over 4 hours, prefer- ably over 6 hours, and more preferable over 8 hours.
• the retention time is over 16 hours.
• retention time means time of the treatment stage.
• the retention time does not in ⁇ clude a filtration time.
• the temperature is over 60
• the temperature is over 70 °C, preferably over 72 °C, more preferable over 73 °C, and most preferable over 75 °C.
• pH level is suffi- cient low during the treatment stage.
• the pH level is under 3.5, preferable between 2 - 3.
• the pH level is under 2.0, pref ⁇ erably between 0.5 - 1.5.
• the pH level which is between 2 - 4 can be used.
• the pH level is between 0.5
• the temperature is be- tween 80 - 130 ° C, preferably 80 - 105 ° C, and the re ⁇ tention time is between 2 - 60 hours, preferably 6 - 30 hours, at the at least one acid treatment stage, e.g. at the acid hydrolysis stage.
• Temperature is be- low glass transition point of lignin.
• the pH is between 2.5 3.5
• temperature is between 65 - 80 ° C, preferably be ⁇ tween 70 - 80 ° C and more preferable about 70 ° C
• retention time is over 1 hour at the acid washing stage. Increasing temperature and/or retention time and/or decreasing pH level dry solid content and fil- terability may be improved.
• the lignin material is treated in the at least one acid treatment stage and the at least one acid treatment stage is optimized by means of process parameters selected from retention time, temperature, pH level, mixing, oxidizing and their combinations.
• process parameters selected from retention time, temperature, pH level, mixing, oxidizing and their combinations.
• combination of selected process parameters is optimized in the at least one acid treatment stage.
• com ⁇ bination of selected process parameters is optimized in each acid treatment stage.
• the acid treatment stage is adjusted by means of process parameters in order to increase low molecular weight lignin fragments. If harsh reaction conditions, e.g. temperature over 70 °C, retention time over 8 hours and pH level between 1 - 1.5, is applied in the acid hydrolysis then low mo ⁇ lecular weight lignin can be obtained with improved yield.
• harsh reaction conditions e.g. temperature over 70 °C, retention time over 8 hours and pH level between 1 - 1.5
• temperature is be ⁇ tween 55 - 70 ° C and pH is between 9 - 10.5.
• temperature is between 55 - 75 ° C and pH is between 9 - 10
• temperature is between 70 - 80 ° C and pH is below 3.5.
• long retention time is used at least in one stage. Alterna ⁇ tively, the long retention time can be used in more than one stage.
• the long retention time can be used at the acid treatment stage, e.g. in the acid washing and/or in the acid hydrolysis, and/or in the pre- treatment step.
• the formed lignin component (3) is filtrated at the filtration stage (4a, 4b) after at least the latest acid treatment stage (2a, 2b) . In one embodiment the formed lignin component is filtrat ⁇ ed after each of the at least one acid treatment stag ⁇ es .
• the filtration refers to any filtration method which can be used in the filtration of the lignin.
• the lignin component is washed by water and pressed and op ⁇ tionally air-dried.
• the filtration can be performed by any suitable filtration device.
• the formed lignin component is filtrated by pressure filtration or vacuum filtration. In one embodiment pressure is between 10 - 20 bar, preferably 13 - 17 bar and more preferable about 15 bar in the pressure filtration .
• the pH level is adjusted just before the filtration, especially if shorter re ⁇ tention time is used in the acid treatment stage.
• temperature is over 50 °C and pH is between 2 to 4 during the filtration.
• the lignin material is treated in the at least one acid treatment stage such that dry solids content of the lignin component can be increased ⁇ 5 preferably 5 - 15 %, more prefera ⁇ ble about 10 - 15 %, as compared with standard lignin component formed by a known acid washing method.
• dry solids content of the lignin compo ⁇ nent is over 60 %, preferably over 70 %, more prefera ⁇ ble between 70 - 90 % and most preferable between 70 - 80 %.
• the lignin material is treated in the at least one acid treatment stage such that carbohydrates content of the lignin component is under 1.0 %, preferably under 0.5 %, more preferable under 0.2 % and most preferable under 0.1 %.
• the lignin material is treated in the at least one acid treatment stage such that ash content of the lignin component is under 1.0 %, preferably under 0.5 %, more preferable under 0.2 % and most preferable under 0.1 %.
• proportion of lignin dis ⁇ solved during the at least one acid treatment stage is adjusted by means of process parameters selected from retention time, temperature, pH level, mixing effi ⁇ ciency, mixer type, oxidation and their combinations. Then low molecular weight lignin component can be achieved. In one embodiment proportion of lignin dis ⁇ solved is adjusted during the acid hydrolysis stage.
• the additional oxidation is made after the filtration in which an acidic filtrate is additionally oxidized.
• the lignin component is ad ⁇ ditionally oxidized during the acid treatment stage, e.g. at the acid hydrolysis stage.
• the additional oxi ⁇ dation may be performed by means of air, oxygen, other oxidizing agent or their combinations in order to sta ⁇ bilize structure of the lignin component, to increase purity of lignin and to remove odour.
• the lignin component (3) obtainable by the method of the present invention can be used as compo- nent in manufacturing a final product selected from activated carbon, carbon fiber, lignin composite, e.g. lignin-plastic composite or lignin-fiber composite, binder material, phenolic component, dispersion agent and their combinations.
• the final product or product comprises the lignin component of the present invention.
• pure lignin component according to the present inven ⁇ tion is needed in the manufacturing of the activated carbon and carbon fibers .
• the method according to the present invention provides the lignin component with good quality. When improving the purify and increasing dry solids content of the lignin component so then it may be provided better properties of the lignin component and the fi- nal product.
• the present invention provides an industrial ⁇ ly applicable, simple and affordable way of making the lignin component from the lignin material.
• the method according to the present invention is easy and simple to realize as a production process.
• the method accord ⁇ ing to the present invention is suitable for use in the manufacture of the different lignin components from different lignin materials.
• a lignin component (3) is formed by an acid treatment.
• a starting lignin material (1) which is flash precipitated lignin, is treated by two acid treatment stages (2a, 2b) .
• the first stage (2a) is an acid washing stage and the second stage (2b) is an ac ⁇ id hydrolysis stage.
• Process conditions are following at the first stage: temperature about 70 ° C, retention time over 1 hour and pH level about 3.
• the acid wash ⁇ ing is performed with H 2 S0 4 .
• Process conditions are following at the second stage: temperature over 70 ° C, retention time over 8 hours and pH level between 1 - 1.5.
• the acid treating in hydrolysis is performed with H 2 S0 4 .
• the lignin component (3) is filtrated after each acid treatment stage (2a, 2b) by pressure filtra ⁇ tion (4a, 4b) . Temperature is over 50 °C and pH is about 2 to 4 during the filtration.
• the lignin component can be additionally oxi ⁇ dized during the acid treatment stage.
• the formed lignin component has low ash and carbohydrates contents. It was discovered that the ash content can be reduced during the first stage. Fur ⁇ ther, the ash content can be still reduced during the second stage. It was discovered that the carbohydrates content can be mainly reduced during the second stage but a part of carbohydrates can be reduced during the first stage.
• high temperature, long reten ⁇ tion time and low pH lignin is softened. After softening, acid is able to hydrolyze carbohydrates and oxi ⁇ dize accessible part of lignin into soluble compounds. Carbohydrates may be removed during the acid treat ⁇ ment .
• dry solids content of the final lignin component cake can be in ⁇ creased and filterability can be enhanced already at the first stage.
• Dry solids content of the lignin com ⁇ ponent can be increased over 5 % as compared with standard lignin component.
• the lignin component has ash content below 0.1 % and carbohydrates content be ⁇ low 0.2 %.
• at least part of inorganic sulphu- re was removed at the acid hydrolysis stage. Further, by means of acid hydrolysis may be increased glass transition temperature of lignin and/or decomposition temperature of lignin.
• lignin struc- ture in the cake of the lignin component was in the form of big-single particles. This explains good fil ⁇ terability and high dry solids content.
• a lignin com ⁇ ponent (3) is formed by an acid treatment.
• a starting lignin material (1) is treated by one acid treatment stage which is an acid washing stage (2a).
• Process conditions are following: tempera ⁇ ture is about 70 ° C, retention time over 1 hour and pH level is about 3.
• the acid washing is performed with H 2 S0 4 .
• the lignin component (3) is filtrated after acid washing by pressure filtration (4a) . Temperature is over 50 °C and pH is about 2 to 4 during the filtration .
• the formed lignin component has low ash content but carbo ⁇ hydrates content has not decreased, such as in example 1. It was discovered that the ash content can be re ⁇ pokerd during the acid washing.
• a lignin component (3) is formed by an acid treatment.
• a starting lignin material (1) is treated by one acid treatment stage which is an acid hydrolysis (2b).
• Process conditions are following: temperature over 70 ° C, retention time over 8 hours and pH level between 1 - 1.5.
• the lignin component (3) is filtrated after acid hydrolysis by pressure filtration (4b) . Tempera ⁇ ture is over 50 °C during the filtration.
• the formed lignin component has low ash and carbohy- drates contents. It was discovered that the ash con ⁇ tent and carbohydrates content can be reduced during the acid hydrolysis.
• a lignin compo ⁇ nent (3) is formed by an acid treatment.
• a starting lignin material (1) is treated firstly at a pre-treatment stage (5) in which is made a re-slurry step, and secondly at an acid washing stage (2a) in order to produce a lignin component. Af- ter the acid washing the lignin component is filtrated (4a) .
• the pre-treatment is car ⁇ ried out so that short retention time and high pH are used. Then, in the acid washing long retention time and low pH are used.
• the pre-treatment is carried out so that long retention time and high pH are used. In the acid washing shorter retention time and low pH, about 2.5, are used. It was discovered that during the pre-treatment of tests 5 and 6 soften ⁇ ing and particle growth of the lignin is happened thanks to long retention time. Therefore, shorter re ⁇ tention time is sufficient in the acid washing.
• T5 is temperature of the pre-treatment
• t5 is retention time of the pre-treatment
• T2a is temperature of the acid washing t2a is retention time of the acid washing
• Tfilt is temperature of the filtration
• a lignin compo ⁇ nent (3) is formed by an acid treatment.
• a starting lignin material (1) is re- slurried, and after then the lignin is treated at an acid treatment stage (2a) in order to produce a lignin component. After the acid treatment the lignin compo ⁇ nent is filtrated (4a) . Delay between the re-slurry and the acid treatment is about 1 hour and temperature is about 60 - 65 ° C.
• Tests 3 - 4 Process conditions of the acid treatment are described in table 2. In the tests 3 - 4 the acid treatment is carried out so that long retention time and low pH are used. Tests 1 and 2 are comparative tests. In test 1 low temperature and short retention time are used. In test 2 low temperature and long re- tention time are used.
• Tfilt is temperature of the filtration
• a lignin compo ⁇ nent (3) is formed by two stage acid treatment.
• a starting lignin material (1) is re- slurried, and after that the lignin is treated at two- stage acid treatment (2a, 2b) in order to produce a lignin component.
• the first acid treatment stage in this example is test 5 in Table 1.
• the first stage is an acid washing and the second stage is an acid hy- drolysis. After each acid treatment stages the lignin component is filtrated (4a, 4b) .
• Lignin cake from the acid washing stage was re-slurried for 1 hour at 60 - 70 °C.
• the pH of the lignin slurry was adjusted just before the acid hy- drolysis stage.
• t2b retention time of the acid hydrolysis
• Tfilt is temperature of the filtration
• Test 9 with T2b of 140 °C, t2b of 1 hour and pH of 3.5 resulted in the formation of char, which adhered to reactor walls.
• a lignin component is formed from a lignin material by an acid treatment, the meth ⁇ od comprising: forming a lignin component (3) of lignin material (1) by treating the lignin material in an acid treatment stage (2) by means of an acid composi- tion; and optimizing process conditions in the acid treatment stage (2) so that high temperature over 70 °C, long retention time, such as delay time, over 6 hours and pH level between 4.5 - 7 are used during the acid treatment in order to remove undesired substance from the lignin component and to purify the lignin component and to reduce acid consumption in the acid treating of lignin.
• the lignin material (1) is treated by an acid washing (2) to form a lignin component (3) .
• the lignin material (1) is treated in an acid washing stage (2) . Long retention time over 6 hours, high temperature over 70 °C, and pH level be ⁇ tween 4.5 and 7 are used in the acid washing.
• the invention is specially based on improving properties of the lignin component.
• the lignin ma ⁇ terial is acid treated by optimizing process conditions and parameters, e.g. retention time and temperature, then higher pH level, e.g. 4.5 - 7 instead of about 2.5, can be used, and then the properties, such as purity, dry solids content and filterability of the lignin com ⁇ ponent are good. Further, acid such as virgin acid con ⁇ sumption can be decreased.
• destabilisation of lignin happens before the filtration thanks to high temperature and long retention time in the acid treat- ment . Further, odour in the lignin component can be de ⁇ creased. Then it is provided the lignin component which is suitable to use in typical and special applications.
• a lignin material refers any material or composition containing lignin.
• the lignin material may contain one or more material components.
• suitable and desired additives can be added into the lignin material to form a desired lignin component.
• the lignin material in ⁇ cludes material which is selected from a group con- sisting of lignin from alkaline pulping process, kraft lignin, lignin from soda process, lignin coming from a process in which lignin is separated the raw material by a solution including suitable chemicals and their combinations .
• the lignin material in ⁇ cludes flash precipitated lignin.
• flash precipitated lignin is obtained after C0 2 - precipitation .
• flash precipitated lignin is formed as disclosed in patent application PCT/FI2011/050896.
• the lignin is precipitated from the black liquor by a continuous process with C0 2 at 6 - 10 bar overpressure.
• the lig ⁇ nin is separated by a flash precipitation lignin sepa- ration method, such as disclosed in patent application PCT/FI2011/050896.
• the lignin is flash precipitated lignin.
• flash precipitated lignin should be understood in this specification as lignin that has been precipi- tated from black liquor in a continuous process by de ⁇ creasing the pH of a black liquor flow, under the influence of an over pressure of 200 - 1000 kPa, down to the precipitation level of lignin using a carbon dioxide based acidifying agent, preferably carbon dioxide, and by suddenly releasing the pressure for precipitat ⁇ ing lignin.
• the residence time in the above method is under 300 s.
• the flash precipitated lignin particles, having a particle diameter of less than 2 ⁇ form agglomerates, which can be separated from black liquor using e.g. filtration.
• the flash precipitated lignin can be purified and/or activated if needed for the further processing.
• the flash precipitated lignin has many advantages, e.g. activity, dispersability, solu ⁇ bility, drainability and preservability.
• the lignin component is a flash precipitated kraft lignin.
• the flash precipitated kraft lignin is undrained.
• There ⁇ fore the lignin has higher activity, and the lignin can be re-dissolved.
• the lignin needs only a very sim ⁇ ple re-dispersing stage when it is added e.g. into an adhesive mixture.
• control of the amount of water in the lignin based composition is easier when the re- dispersing is easier. Further, the lignin is easier to handle in the process because the lignin is not dusty.
• the flash precipitated kraft lignin has dry matter content of 50 - 80 %.
• the lignin material is treated chemically and/or mechanically before the acid treatment stage of the present invention.
• the lignin material is precipitated before the acid treatment stage.
• the lignin ma ⁇ terial is re-slurried before the acid treatment.
• a lignin component means product formed from lignin material in one or more stages.
• Term “lignin component” is already used after the first treatment stage.
• the acid washing refers to any acid washing method.
• the acid washing is performed with an acid composition containing sulphuric acid (H 2 S0 4 ) , other acid or other suita- ble acidifying chemical or their combination.
• H 2 S0 4 sulphuric acid
• the optimization of the process affects positively consump ⁇ tion of H 2 S0 4 or other acid or other acidifying chemical .
• the acid composition con- tains sulphuric acid, which can be virgin acid or re ⁇ cycled acid. Without any process improvements accord- ing to the invention consumption of sulphuric acid is rather high. Sulphuric acid is cheap, but high amount of sodium hydroxide is needed to fulfil Na/S balance of pulp mill. Furthermore, all extra sulphur added to process must be dumped from recovery boiler meaning extra cost.
• the acid composi ⁇ tion contains other acid or other acidifying chemical containing salt.
• Salt can be selected from group K-, Na-, Mg-, A1-, Ca-salt or other suitable salt.
• the acid composition contains sulphate com ⁇ pound with salt.
• the acid composi ⁇ tion contains sodium sesquisulphate .
• Sodium sesquisul- phate (SSS) is a waste fraction from chlorine dioxide plant in pulp mill. In one embodiment waste acid is used as other acid or other acidifying chemical.
• the acid composition contains sul ⁇ phuric acid, and other acid or other acidifying chemical with salt.
• the acid composition contains sulphuric acid and sodium sesquisulphate.
• the acid composition contains sulphuric acid about 10 - 90 w-%, in one embodiment 60 - 70 w-%, and sodium sesquisulphate about 10 - 90 w-%, in one embodiment 30 - 40 w-%.
• the high pH saves acid or oth- er acidifying chemical containing salt which is good for the pulp mill and brings less salt to process, and then less water is needed for washing.
• a suitable combination of temperature, reten- tion time and pH level is selected.
• the selected combi ⁇ nation varies based on acid washing method, lignin mate ⁇ rial, acid composition and desired product.
• long retention time is used in the acid treatment according to the invention.
• the retention time is over 6 hours, prefer- ably over 10 hours, and more preferable between 10 and 20 hours.
• retention time means time of the treatment stage.
• the retention time does not in- elude a filtration time.
• the temperature is over 80 °C during the acid treatment stage, preferably over 85 °C, and more preferable between 80 - 90 °C.
• pH level is suffi- cient high during the acid treatment stage.
• the pH level is over 4.5, preferable over 5.
• the pH level is under 7, preferably under 6.
• the pH level which is between 5 and 6 can be used.
• the pH level is between about 4.5 - 7, preferably about 5 - 6, the temperature is between 70 - 100 ° C, preferably 80 - 90 ° C, and the retention time is over 1 hour, preferably 6 - 30 hours and more preferable between 10 and 20 hours, at the acid treatment stage.
• Increasing temperature and/or retention time and/or pH level dry solid content and filterability may be improved. Improved dry solid content of filter cake leads to lower energy consumption in drying and to lower consumption of water in washing to reach same purity. Also dryer can be smaller, which leads to savings in investment. Savings in water consumption is important, since likely washing water must be circu ⁇ lated back to evaporation plant. Also certain dry solid content is needed to maintain processability of lignin cakes. For applications requiring no drying, for example burning, the low content of water in filter cake is a benefit.
• the method of the invention can be used in connection with any acid treatment process containing one or more acid treatment stages.
• the acid treatment process comprises acid hydrolysis stage before or after the acid washing stage.
• the method of the invention can be used in connection with the acid treatment process described in patent application FI20116253.
• the method of the present in ⁇ vention comprises a pre-treatment step (5) before the acid treatment stage (2) .
• the lignin material is re-slurried in the pre-treatment step.
• the pre-treatment step is a soften ⁇ ing step of lignin in which the lignin is softened and structure of the lignin is modified.
• temperature is between 55 - 70 ° C and pH is between 9 and 10.5.
• long retention time is used at the acid treatment.
• the long retention time can be used also in other stage such as in the pre-treatment stage.
• the long retention time can be used in the acid washing and/or in the pre-treatment step.
• the formed lignin component (3) is filtrated at the filtration stage (4) after the acid treatment stage (2) .
• the filtration refers to any filtration method which can be used in the filtration of the lignin.
• the lig- nin component is washed by water and pressed and op ⁇ tionally air-dried.
• the filtration can be performed by any suitable filtration device.
• the formed lignin component is filtrated by pressure filtration or vacuum filtration. In one embodiment pressure is between 10 - 20 bar, preferably 13 - 17 bar and more preferable about 15 bar in the pressure filtration .
• temperature is over 50 °C and pH is between 5 and 7 during the filtration. In one embodiment the pH level is re-adjusted just before the filtration.
• the process comprises at least two filtration stages. In one embodiment there is one filtration stage after each acid treatment stage. In one embodiment there is the first filtration stage before the acid washing of the invention and the second filtration stage after the acid washing of the invention. In the first filtration stage the lignin material or lignin component washed is filtrated at pH about 10, and then sulphuric acid can be saved in the acid washing.
• the additional oxidation is made after the filtration in which an acidic filtrate is additionally oxidized.
• the lignin component is additionally oxidized during the acid treatment stage.
• the additional oxidation may be per ⁇ formed by means of air, oxygen, other oxidizing agent or their combinations in order to stabilize structure of the lignin component, to increase purity of lignin and to remove odour.
• the lignin component (3) obtainable by the method of the present invention can be used as compo ⁇ nent in manufacturing a final product selected from activated carbon, carbon fiber, lignin composite, e.g. lignin-plastic composite or lignin-fiber composite, binder material, phenolic component, dispersion agent and their combinations.
• the final product or product comprises the lignin component of the present invention.
• pure lignin component according to the present inven ⁇ tion is needed in the manufacturing of the activated carbon and carbon fibers .
• the method according to the present invention provides the lignin component with good quality. When improving the purify and increasing dry solids content of the lignin component so then it may be provided better properties of the lignin product and the final product .
• the present invention provides an industrial ⁇ ly applicable, simple and affordable way of making the lignin component from the lignin material.
• the method according to the present invention is easy and simple to realize as a production process.
• the method accord- ing to the present invention is suitable for use in the manufacture of the different lignin components from different lignin materials.
• a lignin component (3) is formed by an acid treatment on a la- boratory scale.
• a starting lignin material (1) which was flash precipitated lignin, was re-slurred and treated by an acid washing stage (2) .
• Process conditions were following at the acid washing stage: temperature about 87 ° C, retention time about 12 hours and pH level about 5.6.
• the acid washing was performed with an acid composition containing H 2 S0 4 and sodium sesquisulphate (SSS) so that mixture of H 2 S0 4 :SSS was 1:6.
• SSS was 20 % liquid.
• the lignin component (3) was filtrated after the acid washing stage (2) by pressure filtration (4) . Temperature was about 82 ° C and pH was 6.5 - 7 during the filtration. Filtration rate was about 207 kg/m 3 /h. Dry solids content of filter cake was about 78 %.
• lignin struc ⁇ ture in the cake of the lignin component was in the form of big-single particles. This explains good fil ⁇ terability and high dry solids content.
• Example 8 In this example a lignin component (3) is formed by an acid washing according to figure 6 on a pilot scale.
• a starting lignin material (1) which was flash precipitated lignin, was slurred and was treated at an acid washing stage (2) by an acid composition in order to produce a lignin component.
• the acid washing was performed with an acid composition containing H 2 S0 4 and sodium sesquisulphate (SSS) so that mixture of H 2 S0 4 :SSS was 1:6.
• SSS sodium sesquisulphate
• the lignin component (3) was filtrated after the acid washing stage (2) by pressure filtration (4) . Temperature was about 82 ° C and pH was 6.5 - 7 during the filtration.
• Filtration rate is defined during feeding.
• filterability of the lignin component was good even though lignin component was treated in high pH level in the acid washing.
• slurry of the lignin material (1) must stay at pH 5 - 6 for sufficiently long time, over 6 hours and at suffi ⁇ ciently high temperature, over 70 °C, in the acid washing.
• high sodium concentration in the acid washing generally improves filtration, but usually raises final ash con ⁇ tent in lignin component. However, ash content was at an adequate level.
• lignin struc ⁇ ture in the cake of the lignin component was in the form of big-single particles.
• One lignin component of test 2 is shown in figure 8, SEM image. From the all tests of examples 7 - 8 it was discovered that it is important for the invention that long retention time and high temperature together with high pH level are used in the acid washing stage. Fur ⁇ ther, it was important that at least part of sulphuric acid is substituted by other acid or other acidifying chemical with salt. Sulphuric acid consumption can be decreased due to high pH level and substitution of sul ⁇ phuric acid.
• FIG 9. One embodiment of the method of the present in ⁇ vention is shown in figure 9. Another embodiment of the method of the present invention is shown in figure 10.
• FIG 11. One embodiment of the device of the present invention is shown in figure 11.
• a lig- nin component is made from lignin material (1) by an acid treatment.
• a lignin component (3) is formed of lignin material (1) by treating the lignin material by means of an acid com ⁇ position in at least one acid treatment stage (2); and the lignin component is washed and neutralized (6) by a pH-buffer during a filtration (4) after the acid treatment, and pH in pH-buffer is between 4 - 10.
• lignin material refers any material or composition containing lignin.
• the lignin material may contain one or more material components.
• suitable and desired additives can be added into the lignin material to form a desired lignin component.
• the lignin material in ⁇ cludes material which is selected from a group con- sisting of lignin from alkaline pulping process, kraft lignin, lignin from soda process, lignin coming from a process in which lignin is separated the raw material by a solution including suitable chemicals and their combinations .
• the lignin material in ⁇ cludes flash precipitated lignin.
• flash precipitated lignin is obtained after C0 2 - precipitation.
• flash precipitated lignin is formed as disclosed in patent application PCT/FI2011/050896.
• the lignin is precipitated from the black liquor by a continuous process with C0 2 at 6 - 10 bar overpressure.
• the lig ⁇ nin is separated by a flash precipitation lignin separation method, such as disclosed in patent application PCT/FI2011/050896.
• the lignin is flash precipitated lignin.
• flash precipitated lignin should be understood in this specification as lignin that has been precipitated from black liquor in a continuous process by de ⁇ creasing the pH of a black liquor flow, under the in- fluence of an over pressure of 200 - 1000 kPa, down to the precipitation level of lignin using a carbon dioxide based acidifying agent, preferably carbon dioxide, and by suddenly releasing the pressure for precipitat ⁇ ing lignin.
• the residence time in the above method is under 300 s.
• the flash precipitated lignin particles having a particle diameter of less than 2 ⁇ , form agglomerates, which can be separated from black liquor using e.g. filtration.
• the flash precipitated lignin can be purified and/or activated if needed for the further processing.
• the flash precipitated lignin has many advantages, e.g. activity, dispersability, solu ⁇ bility, drainability and preservability .
• the lignin component is a flash precipitated kraft lignin.
• the flash precipitated kraft lignin is undrained.
• There ⁇ fore the lignin has higher activity, and the lignin can be re-dissolved.
• the lignin needs only a very sim ⁇ ple re-dispersing stage when it is added e.g. into an adhesive mixture.
• control of the amount of water in the lignin based composition is easier when the re- dispersing is easier. Further, the lignin is easier to handle in the process because the lignin is not dusty.
• the flash precipitated kraft lignin has dry matter content of 50 - 80 %.
• the lignin material is treated chemically and/or mechanically before the at least one acid treatment stage of the present inven ⁇ tion. In one embodiment the lignin material is precipi ⁇ tated before the at least one acid treatment stage. In one embodiment the lignin material is re-slurried be- fore the at least one acid treatment.
• a lignin component means product formed from lignin material in at one or more stages.
• Term “lignin component” is already used after the first treatment stage.
• the at least one acid treatment stage (2) is selected from a group consist ⁇ ing of acid washing, acid hydrolysis and their combi ⁇ nations.
• the acid treatment (2) is carried at one stage or alternatively at more than one stage.
• the at least one acid treatment stage (2) is acid washing.
• the at least one acid treatment stage (2) is acid hydrolysis.
• the lignin material (1) is treated at two acid treatment stages (2) in which one of stages is acid washing and one of stages is acid hydrolysis.
• the acid washing refers to any acid washing method.
• the acid washing is performed with an acid composition containing sulphuric acid (H 2 S0 4 ) , other acid or other suita- ble acidifying chemical or their combination.
• H 2 S0 4 sulphuric acid
• the optimization of the process affects positively consump ⁇ tion of H 2 S0 4 or other acid or other acidifying chemical .
• the acid hydrolysis refers to any acid hydrolysis method.
• the acid hydrolysis is performed by means of H 2 S0 4 , or oth- er suitable acidifying chemical, typically in the presence of water.
• the acid composition in ⁇ cludes H 2 S0 4 which can be virgin acid or recycled acid. In one embodiment the acid composition includes acidi ⁇ fying chemical.
• a suitable combination of temperature, retention time and pH level is selected.
• the selected combination varies based on acid washing or hydrolysis method, lignin material, acid composition and desired product .
• Any acid treatment process can be used in connection with the present invention, for example ac- id treatment process as disclosed patent application FI20116253 or FI20125703 or other suitable acid treat ⁇ ment method can be used.
• a lignin component is made from lignin material (1) by a mild acid treatment so that the lignin material (1) is treated in at least one acid treatment stage (2) and the at least one acid treatment stage is optimized by means of a combination of process parameters comprising retention time, e.g. long retention time, temperature, e.g. high tempera- ture, and pH level, e.g. sufficient low, in order to decrease ash and/or carbohydrates in the lignin compo ⁇ nent, and preferably in order to remove undesired sub ⁇ stance from the lignin component and to purify the lignin component.
• the lignin compo- nent is formed as disclosed in patent application FI 20116253.
• the method comprising: op ⁇ timizing process conditions in the acid treatment stage so that high temperature, long retention time and low pH level are used during the acid treatment.
• long retention time is used at the acid treatment stage, in at least one acid treat ⁇ ment stage.
• retention time means time of the acid treatment stage. The retention time does not include a filtration time.
• a lignin component is made from lignin material by an acid treatment, the method comprising: forming a lignin component of lignin material by treating the lignin material in at least one acid treatment stage; and optimizing process conditions by means of a combi ⁇ nation of process parameters comprising retention time, temperature and pH level at the acid treatment stage so that the retention time is over 6 hours dur ⁇ ing at least one acid treatment stage.
• the retention time which is over 8 hour is used during the acid treatment. In one embodiment the retention time which is over 10 hour is used during the acid treatment. In one embodiment the retention time which is over 16 hour is used during the acid treatment.
• the temperature which is over 70 °C is used during the acid treatment. In one embodiment the temperature is over 72 °C, more prefer ⁇ able over 73 °C, and most preferable over 75 °C.
• the pH level which is be ⁇ tween 0.5 - 4 is used during the acid treatment. In a preferred embodiment pH level is sufficient low during the treatment stage. In one embodiment the pH level is under 3.5, preferable between 2 - 3. In one embodiment the pH level is under 2.0, preferably between 0.5 - 1.5. In one embodiment the pH level which is between 2 - 4 can be used.
• the method comprises a pre- treatment step before the at least one acid treatment stage.
• the lignin material is re- slurried in the pre-treatment step.
• the pre-treatment step is a softening step of lignin in which the lignin is softened and structure of the lignin is modified.
• long retention time is used at least in one acid treatment stage.
• the long retention time can be used in more than one stage.
• the long retention time can be used at the acid treatment stage, e.g. in the acid washing and/or in the acid hydrolysis, and/or in the pre-treatment step.
• Increasing retention time and/or temperature dry solid content and filterability may be improved. Improved dry solid content of filter cake leads to lower energy consumption in drying and to lower consumption of washing liquid in washing to reach good purify .
• pH in pH-buffer is between 5 - 9. In one embodiment pH in pH-buffer is between 6 8. In one embodiment pH in pH-buffer is over 4, preferably over 5, and more preferable over 6. In one embodiment pH in pH-buffer is below 10, preferably be ⁇ low 9, and more preferable below 8. Highly alkaline washing liquid, in which pH is higher than 10, increases dissolution of lignin rapidly.
• pH-buffer is in the form of solution .
• the pH-buffer may include one or more than one component.
• the pH-buffer contains at least one buffer agent.
• the pH- buffer includes buffer agent selected form a group consisting of citrate, acetate, carbonate and their combinations.
• the pH-buffer includes alkaline based compound, e.g. NaOH. In one embodiment the alkaline based compound is used to adjust pH level in the pH-buffer.
• the pH-buffer includes citrate as a buffer agent.
• the pH-buffer includes citrate and alkaline based com ⁇ pounds and water, and pH of the pH-buffer is between 5 - 7.
• the pH-buffer can include any suitable buffer agent.
• the pH-buffer includes water. Composition of the pH-buffer can be optimized by taken into account the requirements of processes and final products.
• the method of the invention com ⁇ prises the filtrating (4) of the lignin component af ⁇ ter the acid treatment.
• the formed lignin component (3) is filtrated at the filtration stage (4) after at least the latest acid treatment stage (2 ) .
• the filtration refers to any filtration method which can be used in the filtration of the lignin.
• the lignin component is filtrated, washed and pressed and op- tionally air-dried.
• the filtration can be performed by any suitable filtration device.
• the formed lignin component is filtrated by pressure filtration or vacuum filtration. In one embodiment pressure is between 10 - 20 bar, preferably 13 - 17 bar and more preferable about 15 bar in the pressure filtration .
• the filtration comprises a filtrating step, containing feeding of the lignin component, for forming a filter cake and washing step, such as a cake washing step, for washing the filter cake in order to decrease ash content in the lignin product. Further, the filtration may comprise a pre-pressing step before the washing step and a final pressing step after the washing step.
• the lignin component is neutralized during the filtration, preferably in connection with the washing step, such as cake washing step.
• the washing of the lignin component is made by means of the pH-buffer.
• the lignin component is neu ⁇ tralized.
• the pH-buffer is used instead of clean water when washing the filter cake.
• the filtration device (10) comprises a lignin feeding equipment for feeding the lignin component (7) from an acid treat ⁇ ment stage into the filtration device, and a filtrat- ing step for forming a cake of the lignin component and a washing step for washing the cake, and a pH- buffer feeding equipment (9) for feeding the pH-buffer
• the filtration device may com ⁇ prise a pre-pressing step between the filtration step and the washing step and/or a final pressing step af ⁇ ter the washing step.
• (9) may contain one or more than one device selected from the group consisting of tank, pipe, pipeline, tube, pump and their combination or the like to feed the pH-buffer into the washing step.
• the filtration device (10) comprises at least one feeding tank from which pH- buffer or component of the pH-buffer is fed into the washing step, into the pH-buffer feeding equipment or into a mixing device.
• the pH-buffer is fed from the feeding tank into the washing step by means of the pH-buffer feeding equipment.
• the pH-buffer feeding equipment contain at least one feeding tank.
• the pH- buffer is fed from the feeding tank into the washing step .
• the filtration device (10) comprises a mixing device (11) .
• the mixing device contains at least one mixing tank or at least one mixer, e.g. static mixer, in a container or a pipeline in order to form the pH-buffer.
• the pH- buffer may be formed in the mixing device, e.g. in the mixing tank, by combining components of the pH-buffer together and/or by mixing.
• the pH-buffer is fed from the mixing device into the washing step by means of the pH-buffer feeding equipment or via the pH-buffer feeding equipment.
• the forming or mix ⁇ ing of the pH-buffer may be made in the pH-buffer feeding equipment, such as in the pipeline.
• the components of the pH-buffer is fed from the tanks into the feeding equipment for combining the components in the feeding equipment.
• the pH-buffer feeding equipment comprises the mixing device, e.g. static mixer in the pipeline.
• the filtration device (10) comprises an adjustment device to adjust pH of the pH- buffer between 4 to 10, preferably before the washing step.
• pH of pH-buffer is analyzed by an analyzing device.
• the filtration device (10) comprises a controlling means to determine pH of the pH-buffer and/or adjust pH of the pH-buffer between 4 to 10, preferably before the washing step.
• the controlling means comprises at least one analyzing device.
• the con ⁇ trolling means comprises at least one adjustment de ⁇ vice.
• the controlling means compris ⁇ es at least one analyzing device and at least one ad ⁇ justment device.
• the controlling means, adjustment device or analyzing device may be arranged in connec ⁇ tion with the pH-buffer feeding equipment or mixing device. Alternatively, the controlling means, adjust ⁇ ment device or analyzing device may be arranged before the pH-buffer feeding equipment.
• the adjustment device contain means for adding pH-buffer into the washing step and/or means for adding buffer agent into the pH-buffer.
• the ad ⁇ justment device contain at least one adjustable valve for adjusting the feed of the pH-buffer into the washing step.
• the pH-buffer feeding equipment contain at least one adjustable valve for adjusting the feed of the pH-buffer into the washing step wherein the adjustable valve can be adjusted e.g. by means of controlling means or manually.
• the forming of the pH- buffer is made as a batch process. In one embodiment the forming of the pH-buffer is made as a continuous process .
• the filtration device com ⁇ prises feeding tanks, a mixing device containing a mixing tank and a static mixer, and pH-buffer feeding equipment containing a pipeline and pump, and compo ⁇ nents of the pH-buffer from the feeding tanks and wa ⁇ ter are fed into the mixing tank in which the batch of the pH-buffer is formed by mixing with the static mix- er, and the pH-buffer is fed from the mixing device into the washing step by means of the pH-buffer feed ⁇ ing equipment.
• the filtration device com ⁇ prises feeding tanks, pH-buffer feeding equipment con- taining a pipeline and pump, and a mixing device con ⁇ taining a static mixer in connection with the pH- buffer feeding equipment, and components of the pH- buffer from the feeding tanks and water are fed into the pipeline of the pH-buffer feeding equipment in which the pH-buffer is formed by mixing with the static mixer, and the pH-buffer is supplied into the wash ⁇ ing step by the pump.
• components of the pH-buffer and water are not mixed in the pipeline when the pH-buffer is formed.
• the pH-buffer is fed straightly, e.g. a feeding tank, into the washing step by means of the pH-buffer feeding equipment containing pipeline and pump.
• temperature is over 50 °C during the filtration (4) .
• pH of the lignin component is be ⁇ tween 4 - 8 after the filtration (4), in one embodiment between 5 - 7. In one embodiment pH of the lignin component is over 5, in one embodiment over 6. In one embodiment pH of the lignin component is below 8, in one embodiment below 7. In a preferred embodiment pH of the lignin component is about 7.
• the lignin component is dried after the filtration.
• the invention relates the lignin component which has specific properties, such as high particle size.
• the lignin component has specific surface area between 0.1 - 1.0 m 2 /g, prefera ⁇ bly between 0.2 - 0.7 m 2 /g, and more preferable be- tween 0.3 - 0.6 m 2 /g.
• a particle size correlates with a specific sur ⁇ face area.
• the lignin component has parti ⁇ cle size which is bigger than in typical lignin products .
• the lignin component is dried and/or grinded after the filtration.
• the lignin component which is dried and grinded into fine particles has bulk density between 200 - 800 g/cm 3 , preferably between 300 - 700 g/cm 3 , more preferable between 400 - 600 g/cm 3 , and in one embodiment about 500 g/cm 3 .
• the bulk density is determined so that the lignin component is dried and grinded into fine particles, and after that the grinded lignin component is put into flexible in ⁇ termediate bulk container, from which a sample is tak- en, and the bulk density of the lignin component is measured from the sample.
• the bulk density of the lignin component of the present invention is bigger than in typical lignin products known in the art .
• the invention relates the lignin component which is formed from lignin material by an acid treatment, wherein a lignin component is formed of lignin material so that the lignin material is treated by means of an acid composition in at least one acid treatment stage; and the lignin component is washed and neutralized by a pH-buffer during a filtra ⁇ tion after the acid treatment, and pH in pH-buffer is between 4 - 10.
• ash content of the lignin compo- nent is low.
• the invention relates a use of the lignin component obtainable by the method of the in ⁇ vention, wherein the lignin component is used as component in manufacturing a final product selected from a group consisting of activated carbon, carbon fiber, lignin composite, binder material, phenolic component, dispersion agent and their combinations.
• the invention relates a product which includes the lignin component obtainable by the method of the invention.
• the prod ⁇ uct is selected from a group consisting of activated carbon, carbon fiber, lignin composite, e.g. lignin- plastic composite or lignin-fiber composite, binder material, phenolic component, dispersion agent and their combinations.
• the invention is specially based on improving properties of the lignin component.
• the properties e.g. purity, dry solids con ⁇ tent, filterability, amounts of carbohydrates and ash, of the lignin component can be improved. Further, odour in the lignin component can be decreased.
• the lignin component is neutralized then the neutral lignin component can be achieved. Then it is provided the lignin component which is suitable to use in typical and special applications.
• the method according to the present invention provides the neutral lignin component with good quali ⁇ ty, such as purify and dry solid content.
• good quali ⁇ ty such as purify and dry solid content.
• the neutral lignin component is non-corrosive. Then additional pro ⁇ cess stages are not needed to neutralize lignin, when clean water is replaced by pH-buffer during the washing. Neutralization of the lignin product in additional pro ⁇ cess stage is extremely difficult since after the sepa ⁇ rate neutralization stage a dewatering of the lignin product is difficult to make. The production of neutral lignin is necessity for most applications. Further, even burning of the lignin component benefits from non- corrosive nature of this biofuel. Non-corrosive lignin component can be fed in application process without need for stainless/acid-proof steel as material in feeding systems. Also, standard material can be used in storage silos. Further, neutral lignin is less harmful to health .
• the present invention provides an industrial ⁇ ly applicable, simple and affordable way of making the lignin component from the lignin material.
• the method according to the present invention is easy and simple to realize as a production process.
• the method accord ⁇ ing to the present invention is suitable for use in the manufacture of the different lignin components from different lignin materials.
• a lignin component (3) is formed by an acid treatment.
• a starting lignin material (1) which is flash precipitated lignin, is treated by one acid treatment stage (2) which is an acid washing stage.
• Process conditions are following: temperature is about 70 ° C, retention time over 6 hour and pH level is about 3. The acid washing is performed with H 2 S0 4 .
• the lignin component (3) is filtrated after the acid washing (2) by pressure filtration (4) . Temperature is over 50 °C during the filtration. During the filtration (4), the washing and neutralization (6) of the lignin component is made by pH-buffer solution (8) containing citrate, acetate and/or carbonate as a buffer agent. pH of the pH-buffer solution is about 5
• the neutral lignin component is achieved.
• the lignin component has specific surface area between 0.1
• Example 10 In this example and in figure 10, a lignin component (3) is formed by an acid treatment.
• a starting lignin material (1) which is flash precipitated lignin, is treated firstly at a pre-treatment stage 5 in which a re-slurry step and filtration are made, and then at one acid treatment stage (2) which is an acid washing stage.
• Process con ⁇ ditions are following: temperature is about 70 ° C, re ⁇ tention time over 6 hour and pH level is about 3.
• the acid washing is performed with H 2 S0 4 .
• the lignin component (3) is filtrated after the acid washing (2) by pressure filtration (4) . Temperature is over 50 °C during the filtration.
• the washing and neutralization (6) of the lignin component is made by pH-buffer solution (8) containing citrate, acetate and/or carbonate as a buffer agent. pH of the pH-buffer solution is about 6
• the neutral lignin component is achieved.
• the lignin component has specific surface area between 0.2
• a lignin component (7) formed by an acid treatment is filtrated by pressure filtration (4) . Temperature is over 50 °C during the filtration.
• the washing and neutralization (6) of the lignin component is made by pH-buffer solution containing citrate as a buffer agent. pH of the pH-buffer solution is about 6
• the filtration, washing and neutralization is carried out in a filtration device (10) .
• the filtra ⁇ tion device (10) comprises a lignin feeding equipment for feeding the lignin component into the device, a filtrating step for forming a cake of the lignin com- ponent, a washing step for washing the cake and a fi ⁇ nal pressing step for pressing.
• the filtration device may comprise a pre-pressing step be ⁇ tween the filtration step and the washing step.
• a lig- nin component product (3) is formed during the filtra ⁇ tion.
• the pH-buffer solution is formed from buffer agent (12a) containing citrate agent, NaOH (12b) and water (13) by mixing in a mixing device (11) compris- ing a mixing tank or a mixer in a container or a pipeline.
• the pH-buffer solution (8) is fed by pH-buffer feeding equipment (9) containing a feeding pipeline and a pump into a washing step of the filtration de ⁇ vice (10) for washing and neutralizing a cake of the lignin component (7) .
• the mixing of the pH-buffer solution may be made in the feeding equipment, such as in the pipeline.
• the lignin component (3) may be dried and grinded .
• pH of the lignin component product is determined after the filtration.
• the pH is measured from the lignin components of the present in- vention and reference samples.
• the lignin components of the present inven ⁇ tion have been formed by means of examples 9 and 11. During the filtration the lignin products washed by the pH-buffer in which pH was 6. The pH-buffer con- tained citrate agent (2.1 g/1 citric acid), NaOH (pH 6) and water.
• the reference samples have been formed by similar means than trial points. During the filtration the lignin products were washed by clean water.
• pH of the lignin compo ⁇ nent can be increased by means of the method according to the present invention in comparison with reference samples .
• lignin struc ⁇ ture in the cake of the lignin component was in the form of big-single particles. This explains good fil ⁇ terability and high dry solids content.
• the invention relates the lignin component which has specific properties, such as high particle size.
• the lignin component has specific surface area between 0.1 - 1.0 m 2 /g, prefera ⁇ bly between 0.2 - 0.7 m 2 /g, and more preferable be ⁇ tween 0.3 - 0.6 m 2 /g.
• a particle size correlates with a specific sur- face area.
• the lignin component has parti ⁇ cle size which is bigger than in typical lignin products .
• the lignin component is dried .
• the lignin component is dried and/or grinded after the filtration.
• the lignin component which is dried and grinded into fine particles has bulk density between 200 - 800 g/cm 3 , preferably between 300 - 700 g/cm 3 , more preferable between 400 - 600 g/cm 3 , and in one embodiment about 500 g/cm 3 .
• the bulk density is determined so that the lignin component is dried and grinded into fine particles, and after that the grinded lignin component is put into flexible in- termediate bulk container, from which a sample is taken, and the bulk density of the lignin component is measured from the sample.
• the bulk density of the lignin component of the present invention is bigger than in typical lignin products known in the art.
• Example 13 specific surface areas of lignin components are determined from the lignin com ⁇ ponent of the present invention and reference samples.
• the lignin components of the present inven- tion have been formed by means of an acid treatment according to the present invention in which is used long retention time, over 6 h, and temperature over 70 °C.
• the reference samples have been formed by means of a typical acid treatment process in which is used low temperature and short retention time.
• the lignin component of the present invention has particle size which is bigger than in typical lig- nin products.
• the ash content and carbohydrates content can be reduced during the acid hydrolysis without major influence on structure of lignin. It is well known from the prior art that the carbohydrates can be removed from lignin using strong acid hydrolysis, but this will result in charring of lignin. Thanks to the invention the carbohydrates can be removed from lignin using mild conditions in the acid hydrolysis .
• lignin product has pH of 2.5, so an addi ⁇ tional process stage may be needed to neutralize lignin product when close to neutral lignin is required in some downstream processing or applications. Separate neutral ⁇ ization stage would bring significant additional cost to process, since filtering of close to neutral lignin slurry is extremely slow by using standard methods. Clearly lower dry solids content of filter cake obtained after standard neutralization stage has biggest effect on raised operating costs. Thanks to the embodiments of the invention the neutral lignin product can be formed without separate neutralization stages.
• the method according to the present invention is suitable in different embodiments to be used for making the most different kinds of lignin components from different lignin materials.
• the lignin component according to the present invention is suitable in dif ⁇ ferent embodiments to be used in different final prod ⁇ ucts .

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